IL-6 和 IL-10 基因序列与儿童热性惊厥的关系

Merwa A. Raheem, Prof.Dr. Ibrahim A. Altamemi
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引用次数: 0

摘要

背景:发热性惊厥通常是指 6 个月至 5 岁的儿童在发烧超过 38 摄氏度时发生的惊厥,与感染、头部受伤或癫痫等颅内原因无关。这也被称为未成熟大脑对发烧的反应,与年龄有关。随着儿童大脑的发育,神经元的兴奋性会增加,从而使儿童面临发热性癫痫发作的风险。目的:本研究旨在找出炎性细胞因子(IL-6、IL-10)SNP 与儿童发热性癫痫发作的关系。方法:在无菌条件下采集儿童热性惊厥患者的血样,利用等位基因特异性 PCR 技术研究 IL-6 (-597) G/A 和 IL-10 (-819) C/T 的 SNP 与疾病易感性的关系。研究结果对 40 名发热性癫痫发作患者和 40 名无发热性癫痫发作的对照组进行的病例对照研究显示,患者组和对照组之间 IL-6 基因型的频率分布存在显著差异(P =0.041)。此外,IL-10 基因型和等位基因的频率分布没有明显差异。(P>0.05);因此,任何基因型或等位基因都不能被视为危险因素或保护因素。结论本研究得出结论,IL-6(-597) G/A, (rs:1800797) 单核苷酸多态性(SNP)与热性惊厥易感性相关,GG 基因型被认为是危险因素,而 GA 基因型则是保护因素。然而,IL-10-819C/T(rs:1800871)基因可能并不代表与发热性癫痫发作相关的遗传风险因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association Of IL-6, And IL-10 Gene Snps In Childhood Febrile Seizure
Background: Febrile seizure are typically defined as convulsions=that-occur in children, between/6 months to 5years, who have a fever of more,,than”38 degrees Celsius, that is not associated with an intracranial’ reason such as an infection, ,head .injury, or epilepsy. It is also known as the immature brain's response to fever, which is age-dependent. As a child’s brain develops, there is an increase in neuronal excitability which puts the child at the risk of febrile seizures. Aims: the aim of the present study is to find out the association of Inflammatory cytokines (IL-6, IL-10) SNP with the onset of childhood febrile seizure. Method- Blood samples from patients with childhood febrile seizure will be collected in a sterile condition, and the association of SNP for both IL-6 (-597) G/A, and IL-10 (-819) C/T with disease susceptibility will be studied by using allele specific PCR. Results: The case-control study of 40 patients with Febrile seizure and 40 control without Febrile seizure has revealed that a substantial difference in the frequency distribution of IL-6 genotypes between the patient group and the control group where (p =0.041). Besides, there was no discernible variation in the frequency distribution of IL-10 genotypes and alleles. (p > 0.05); therefore, none of genotypes or alleles can be regarded as risk factor or protective factor. Conclusion: The present study has concluded that IL-6(-597) G/A, (rs:1800797) single nucleotide polymorphism (SNP) was associated with Febrile seizure susceptibility, and GG, genotype considered as, risk factor, while genotype GA act as protective factor. However, it refers that the IL-10-819C/T (rs:1800871), genes may not represent the  Febrile-seizure-associated genetic risk factor.
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